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HRID 718657作成日:2026年10月25日

Ethyl Acetate → Ethyl 1-(4-nitrophenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/718657

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物p-FluoronitrobenzeneHCID 9590—
反応物Potassium CarbonateHCID 11430—
反応物Ethyl 4-piperidinecarboxylateHCID 70770—
溶媒Dimethyl SulfoxideHCID 679—
生成物Ethyl 1-(4-nitrophenyl)piperidine-4-carboxylateHCID 2796870—

反応条件

温度100 °C

反応手順

To a solution of 1-fluoro-4-nitrobenzene (3.0 g, 21 mmol) in DMSO (30 mL) was added ethyl piperidine-4-carboxylate (5.0 g, 32 mmol) and K2CO3 (5.9 g, 43 mmol). The resulting mixture was stirred at 100° C. for 8 h, and allowed to cool to rt. EtOAc (300 mL) was added. The organic layer was washed with water (3×100 mL) and brine, dried over Na2SO4, filtered and concentrated to give a residue, which was purified by flash column chromatography on silica gel (EtOAc/petroleum ether (1:2 v/v)). Compound 54a was obtained as a yellow solid. Mass Spectrum (LCMS, ESI pos.): Calcd. for C14H18N2O4: 279.1 (M+H). Found 279.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09193736B2
出典データセットuspto-grants-2015_11
ORD IDord-b1800928c0234e3b85156ee5af7b17f6
出典メモuspto-grants-2015_11